19-9214327-C-T
Variant summary
Our verdict is Likely benign. The variant received -2 ACMG points: 2P and 4B. PM2BP4_Strong
The NM_001005191.3(OR7D4):c.511G>A(p.Gly171Ser) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. 16/22 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Uncertain significance (★).
Frequency
Consequence
NM_001005191.3 missense
Scores
Clinical Significance
Conservation
Publications
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ACMG classification
Our verdict: Likely_benign. The variant received -2 ACMG points.
Variant Effect in Transcripts
ACMG analysis was done for transcript: NM_001005191.3. You can select a different transcript below to see updated ACMG assignments.
Ensembl Transcripts
| Sel. | Gene | Transcript | Tags | HGVSc | HGVSp | Effect | Exon Rank | Protein | UniProt |
|---|---|---|---|---|---|---|---|---|---|
| OR7D4 | MANE Select | c.511G>A | p.Gly171Ser | missense | Exon 2 of 2 | ENSP00000493383.1 | Q8NG98 | ||
| OR7D4 | TSL:6 | c.511G>A | p.Gly171Ser | missense | Exon 1 of 1 | ENSP00000310488.2 | Q8NG98 | ||
| OR7D4 | c.511G>A | p.Gly171Ser | missense | Exon 2 of 2 | ENSP00000493404.1 | Q8NG98 |
Frequencies
GnomAD3 genomes Cov.: 32
GnomAD4 exome Cov.: 33
GnomAD4 genome Cov.: 32
ClinVar
Computational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at